Aline R F, Myler P J, Stuart K D
Seattle Biomedical Research Institute, Washington 98109-1651.
Exp Parasitol. 1989 Jan;68(1):8-16. doi: 10.1016/0014-4894(89)90003-9.
We have observed the loss of an inactive telomeric variant surface glycoprotein (VSG) gene that is located on a minichromosome in Trypanosoma brucei. If this is due to gene conversion, it is the third "silent" gene conversion (i.e., one that does not produce an antigenic switch) detected in 19 antigenic switches of the IsTaR 1 serodeme. This is surprisingly frequent since the immune response cannot select against the inactive gene. We estimate that 10(-1) to 10(-3) telomeric VSG gene conversions occur per generation, which is at least 100 times more frequent than antigenic switching. Since all three "silent" gene conversions involved an IsTat 5 VSG gene, the frequency may vary among telomeric VSG genes. However, the high gene conversion frequency for the 5 VSG gene does not ensure a higher antigenic switch frequency than other telomeric VSG genes for which we have probes. These results suggest that gene conversion rapidly alters the repertoire of telomeric VSG genes, possibly including those on minichromosomes, producing a continual variation in the VSG genes that are more likely to be expressed.
我们观察到布氏锥虫的一个位于微型染色体上的无活性端粒可变表面糖蛋白(VSG)基因缺失。如果这是由于基因转换导致的,那么这是在IsTaR 1血清型的19次抗原转换中检测到的第三次“沉默”基因转换(即不产生抗原转换的基因转换)。这一情况出人意料地频繁,因为免疫反应无法针对无活性基因进行选择。我们估计每代发生10⁻¹至10⁻³次端粒VSG基因转换,这比抗原转换的频率至少高100倍。由于所有三次“沉默”基因转换都涉及IsTat 5 VSG基因,不同端粒VSG基因的转换频率可能有所不同。然而,5 VSG基因的高基因转换频率并不意味着其抗原转换频率高于我们拥有探针的其他端粒VSG基因。这些结果表明,基因转换会迅速改变端粒VSG基因库,可能包括微型染色体上的基因,从而使更有可能表达的VSG基因不断发生变化。